K-number	K101471
Device name	AXLE INTERSPINOUS FUSION SYSTEM
Applicant	X-Spine Systems, Inc.
Product code	KWP
Device class	Class II
Decision date	Nov 24, 2010
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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AXLE INTERSPINOUS FUSION SYSTEM

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